References

 

1)      Bezzina, Connie., et al. “Compound Heterozygosity for Mutations (W156X and R225W) in SCN5A Associated With Severe Cardiac Conduction Disturbances and Degenerative Changes in Conduction Systems.” Circulation Research 2003 Feb 7; 92(2):159-68.

      http://circres.ahajournals.org/cgi/content/abstract/92/2/159

 

2)      Cardio Update. “Long QT syndrome.” 2002. Sibley Heart Center Cardiology.

      http://www.choa.org/cardiology/cardio-update/fall2002.shtml

 

3)      Clancy. Colleen E., et al. “Insights into the molecular mechanisms of bradcardia-triggered arrhythmias in long QT3 syndrome.” The Journal of Clinical Investigation. 2002 Nov. Vol 110.

 

4)      “Long QT Syndrome (LQT).” Cleveland Clinic Heart Center. 3 May 2003.

      http://www.clevelandclinic.org/heartcenter/pub/guide/disease/electric/longqtsyndrome.htm?index=10494

 

5)      Marx, Jean. “Gene Mutation May Boost Risk of Heart Arrhythmias.” Science Magazine. Vol 297. (2002): 23 Aug. 2002.

      www.sciencemag.org

 

6)      Neuromuscular Disease Center. ION CHANNELS, TRANSMITTERS, RECEPTORS & DISEASE. 10 Feb 2000.

       http://www.neuro.wustl.edu/neuromuscular/mother/chan.html

 

7)      QTsyndrome.ch. 2002.

      http://www.qtsyndrome.ch

 

8)      Online Mendelian Inheritance in Man. LONG QT SYNDROME 3; LQT3. 5 Feb 2003. NCBI.

      http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603830

 

9)      Ravina, Thomas. Lapuerta, Jose A. and Brugada, Josep.  “Prolonged repolarization in long QT3 syndrome: unusual electrocardiographic findings.” International Journal of Cardiology 82 (2002): 71-73.

 

10)  Splawski, Igor., et al. “Variant of SCN5A Sodium Channel Implicated in Risk of Cardiac Arrhythmia.” Science Magazine. Vol 297 23 Aug. 2002

 

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